Till startsida
Sitemap
To content Read more about how we use cookies on gu.se

Kalliopi Sofou

Resercher

Kalliopi Sofou
Resercher
kalliopi.sofou@vgregion.se
+46 31-343 6416

Postal Address: Rondvägen 10, 416 85 Göteborg
Visiting Address: Rondvägen 10 , 41685 Göteborg


Department of Pediatrics at Institute of Clinical Sciences (More Information)
Drottning Silvias Barn O ungdomsjukh
416 85 Göteborg
Visiting Address: Drottning Silvias Barn O ungdomsjukh , 416 85 Göteborg

Latest publications

Responding to feedback on the SITUPS mnemonic for medical students
Kristina Bry, Kalliopi Sofou
Acta Paediatrica, International Journal of Paediatrics, Editorial letter 2020
Editorial letter

KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia
M. Pennings, M. I. Schouten, J. van Gaalen, R. P. P. Meijer, S. T. de Bot et al.
European Journal of Human Genetics, Journal article 2020
Journal article

Phenotype-genotype correlations in Leigh syndrome: new insights from a multicentre study of 96 patients.
Kalliopi Sofou, Irenaeus F M de Coo, Elsebet Ostergaard, Pirjo Isohanni, Karin Naess et al.
Journal of medical genetics, Journal article 2018
Journal article

Ketogenic diet in pyruvate dehydrogenase complex deficiency: short- and long-term outcomes.
Kalliopi Sofou, Maria Dahlin, Tove Hallböök, Marie Lindefeldt, Gerd Viggedal et al.
Journal of inherited metabolic disease, Journal article 2017
Journal article

Showing 1 - 10 of 22

2020

Responding to feedback on the SITUPS mnemonic for medical students
Kristina Bry, Kalliopi Sofou
Acta Paediatrica, International Journal of Paediatrics, Editorial letter 2020
Editorial letter

KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia
M. Pennings, M. I. Schouten, J. van Gaalen, R. P. P. Meijer, S. T. de Bot et al.
European Journal of Human Genetics, Journal article 2020
Journal article

2019

2018

Phenotype-genotype correlations in Leigh syndrome: new insights from a multicentre study of 96 patients.
Kalliopi Sofou, Irenaeus F M de Coo, Elsebet Ostergaard, Pirjo Isohanni, Karin Naess et al.
Journal of medical genetics, Journal article 2018
Journal article

2017

Ketogenic diet in pyruvate dehydrogenase complex deficiency: short- and long-term outcomes.
Kalliopi Sofou, Maria Dahlin, Tove Hallböök, Marie Lindefeldt, Gerd Viggedal et al.
Journal of inherited metabolic disease, Journal article 2017
Journal article

2016

Showing 1 - 10 of 22

Page Manager: Katarina Olinder Eriksson|Last update: 10/1/2013
Share:

The University of Gothenburg uses cookies to provide you with the best possible user experience. By continuing on this website, you approve of our use of cookies.  What are cookies?